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Updated: May 25, 2025

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Published on: September 20, 2021
Sulfide-Responsive Transcription Control in Escherichia coli
Koichi Hori1, Rajalakshmi Balasubramanian1, Shinji Masuda1,2
1School of Life Science & Technology, Tokyo Institute of Technology, Yokohama 226-8501, Japan.
Sulfide influences gene expression in Escherichia coli through YgaV-dependent and independent pathways. YgaV acts as a global regulator, controlling redox homeostasis by repressing and activating transcription.
Area of Science:
- Microbiology
- Molecular Biology
- Genomics
Background:
- Sulfide significantly impacts microbial physiology and gene expression.
- The transcription factor YgaV is implicated in sulfide response in Escherichia coli.
- Understanding transcriptional regulation is crucial for microbial adaptation.
Purpose of the Study:
- To elucidate the mechanism of large-scale transcriptional changes induced by sulfide in Escherichia coli.
- To investigate the role of transcription factor YgaV in sulfide-mediated gene regulation.
- To determine if YgaV functions as a global regulator involved in redox homeostasis.
Main Methods:
- Large-scale RNA-sequencing was performed on wild-type and YgaV deletion mutant Escherichia coli.
- Cultures were grown under aerobic, semi-aerobic, and semi-aerobic with sulfide conditions.
- Principal component analysis was used to categorize gene expression data.
Main Results:
- Gene expression patterns were categorized into five principal components.
- Identified transcriptional mechanisms dependent on sulfide but independent of YgaV.
- Identified transcriptional mechanisms dependent on YgaV but independent of sulfide.
- YgaV functions as both a transcriptional repressor and activator.
Conclusions:
- YgaV plays a dual role in transcriptional regulation, acting as both an activator and repressor.
- These findings support the hypothesis that YgaV is a global regulator essential for maintaining redox homeostasis in Escherichia coli.
- Sulfide-induced transcriptional changes involve both YgaV-dependent and YgaV-independent pathways.
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